Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Congenital short bowel.

C M Tiu, Y H Chou, H B Pan

    Pediatric Radiology
    |January 1, 1984
    PubMed
    Summary
    This summary is machine-generated.

    Congenital short bowel without atresia, a rare condition, was observed in two male siblings. This report reviews this anomaly and four previously documented cases in medical literature.

    Related Concept Videos

    You might also read

    Related Articles

    Articles linked to this work by shared authors, journal, and citation graph.

    Sort by
    Same author

    [Research progress on the mechanism of mitochondrial dynamics in diabetic foot ulcers and its related intervention strategies].

    Zhonghua shao shang yu chuang mian xiu fu za zhi·2026
    Same author

    Virtual reality for training emergency medicine residents in emergency scenarios: usefulness of a tutorial to enhance the simulation experience.

    Frontiers in digital health·2025
    Same author

    Rituximab induced cerebral venous sinus thrombosis in a patient with anti-N-methyl-D-aspartate receptor-antibody encephalitis: a case report and review of literature.

    Journal of medical case reports·2024
    Same author

    Performance of neuroretinal rim thickness measurement by Cirrus high-definition optical coherence tomography in myopic eyes.

    Scientific reports·2023
    Same author

    Double Stress Overshoot in Start-Up of Simple Shear Flow of Entangled Comb Polymers.

    ACS macro letters·2022
    Same author

    Research Note: Orange corn altered the cecal microbiome in laying hens.

    Poultry science·2022
    Same journal

    Head-to-head comparison of [<sup>18</sup>F]-mFBG versus [<sup>123</sup>I]-MIBG in neuroblastoma: a systematic review and meta-analysis.

    Pediatric radiology·2026
    Same journal

    Comment on "super-resolution MRI-derived brainstem and cerebellar volumes in fetuses between 22 weeks and 32 weeks of gestation".

    Pediatric radiology·2026
    Same journal

    Ferumoxytol dose optimization for three-dimensional whole-heart magnetic resonance imaging in patients with congenital heart disease.

    Pediatric radiology·2026
    Same journal

    Widely available, general-purpose generative AI applications for radiology education: determining the teaching quality of synthetic pediatric neuroradiology images.

    Pediatric radiology·2026
    Same journal

    Sustainability: a physician's cautionary tale.

    Pediatric radiology·2026
    Same journal

    The invisible footprint: why planetary health is a pediatric radiologist's obligation.

    Pediatric radiology·2026
    See all related articles

    Area of Science:

    • Pediatric Surgery
    • Gastroenterology
    • Medical Genetics

    Background:

    • Congenital short bowel is a rare condition characterized by a shortened small intestine.
    • Malrotation or nonrotation of the bowel can occur with congenital short bowel.
    • The absence of atresia in these cases makes the condition exceptionally rare.

    Observation:

    • Two male siblings presented with congenital short bowel, malrotation/nonrotation, and absence of atresia.
    • This specific combination of anomalies is exceedingly uncommon in pediatric cases.
    • The current report adds to the limited existing literature on this condition.

    Findings:

    • The study details the clinical presentation and management of two affected siblings.
    • A review of four previously reported cases in English literature was conducted.

    Related Experiment Videos

  • The findings highlight the rarity and specific characteristics of this congenital anomaly.

    • Implications:

    • Understanding this rare anomaly is crucial for accurate diagnosis and appropriate management in affected infants.
    • Further research may elucidate the genetic or environmental factors contributing to this condition.
    • This case series contributes valuable data to the limited knowledge base, aiding future clinical practice and research.